A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566185



Internal ID16353594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105194429..105219528hg38UCSC Ensembl
Innerchr14:105660766..105685865hg19UCSC Ensembl
Innerchr14:104731811..104756910hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3825100
hg1925100
hg1825100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834766
Samples
Known GenesBRF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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